Background
Methods
Aim
Study selection process
i. Mental health nurs$ [mp] OR psychiatric nurs$ [mh,mp] ii. Severe mental illness [mp] OR mental disorders [mh] OR mental illness [mp] OR schizo$ [mh,mp] OR bipolar disorder [mh] OR psychos?s [mp] OR psychotic [mp] OR psychotic affective disorders [mh] OR psychotic disorders [mh] OR psychotic depression [mp] iii. Patient admission [mh] OR patient readmission [mh] OR hospital admission [mp] OR hospital readmission [mp] OR unplanned readmission [mp] OR hospitali?ation [mp] OR readmission rate [mp] OR length of stay [mh] OR emergency department presentation [mp] OR admission to home treatment [mp] OR access to crisis intervention [mp] OR drop-in treatment [mp] OR drop-in care [mp] OR drop-in unit [mp] OR drop-in centre [mp] OR home intervention [mp] OR home therapy [mp] OR home care services [mh] OR home management [mp] iv. Observational study [mh] OR cross-sectional studies [mh] OR cohort studies [mh] OR longitudinal studies [mh] OR epidemiologic studies [mh] OR case-control studies [mh] OR controlled clinical trial [mh] OR randomized controlled trial [mh] OR non-randomised controlled trials as topic [mh] OR quasi-experimental study [mp] OR clinical trial [mh] OR comparative study [mh] v. i AND ii AND iii AND iv |
Outcomes
Data extraction
Risk of bias
Data synthesis
Registration and reporting guidelines
Results
Search results
Description of studies
Authors | Country | Study design (duration) | Setting | Intervention | Control | Study population | Outcomes |
---|---|---|---|---|---|---|---|
Barr et al. [26] | England | Observational study (3 years) | Six general practices (one randomly selected practice from each health locality in an English health district) | Community mental health nurse contact with patients on the severe and enduring mental illness registers of included general practices | No contact with a community mental health nurse | N = 274 Inclusion criteria: participants with severe and enduring mental illness (SEMI), listed on the SEMI register of included general practices Exclusion criteria: not stated Mean age: 45.4 ± 12.2 years Gender: not specified Dropouts: not applicable | Admission to psychiatric hospital, frequency of community mental health nurse contacts |
England | Randomised controlled trial with two parallel arms (18 months) | Community setting within the Greenwich health authority | Community support team (comprising three community psychiatric nurses (CPNs), a team leader and four unqualified mental health workers). Each CPN acted as a care manager/client advocate. [None of the unqualified mental health workers provided services to the research group of 41 clients.] | Generic team (comprising six generic CPNs who worked independently, but were often attached to GP practices). | N = 82 Inclusion criteria: patients with a psychotic disorder (schizophrenia or affective psychosis) lasting more than 2 years, at least 2 hospital admissions in the previous 2 years, aged 18–64 years, living in the Greenwich health district Exclusion criteria: patients with primary organic disorders Mean age: 37 ± 11 years Gender: 56.1% male Dropouts: 10 (24%) patients in the intervention group and 14 (34%) patients in the control group dropped out, for the following reasons: 20 refused to participate, 2 moved away, 1 could not be found and 1 was in prison | Health service use, Global Adjustment Scale, Present State Examination, Brief Psychiatric Rating Scale, Social Adjustment Scale, patient and carer satisfaction, health service costs, accommodation costs, community psychiatric nurse costs |
Description of participants
Description of interventions
Description of outcomes
Assessment of risk of bias
Study | Risk Of Bias In Non-randomised Studies of Interventions (ROBINS-I) tool (for observational studies) | ||||||
Confounding | Participant selection | Intervention classification | Co-intervention | Missing data | Outcome measurement | Selective reporting | |
Barr et al. [26] | High risk | Moderate risk | Moderate risk | Moderate risk | Moderate risk | Moderate risk | Moderate risk |
Study | Cochrane risk of bias tool (for randomised controlled trials) | ||||||
Sequence generation | Allocation concealment | Blinding (participants/personnel) | Blinding (outcome assessors) | Objective outcome | All outcomes reported | Possible biases | |
Unclear risk | Unclear risk | Unclear risk | Unclear risk | Low risk | Low risk | High risk |